240
Participants
Start Date
July 11, 2012
Primary Completion Date
February 26, 2020
Study Completion Date
February 26, 2020
5-FU
Participants will receive 5-FU 400 mg/m\^2 IV q2w.
Atezolizumab
Participants will receive IV atezolizumab (800 mg q2w or 1200 mg q3w) q3w.
Bevacizumab
Participants will receive bevacizumab 10 mg/kg or 15 mg/kg IV q3w.
Carboplatin
Participants will receive carboplatin IV q3w with target AUC of 6 mg/mL.
Leucovorin
Participants will receive leucovorin 400 mg/m\^2 IV q2w.
Nab-paclitaxel
Participants will receive nab-paclitaxel 100 mg/m\^2 IV qw.
Oxaliplatin
Participants will receive oxaliplatin 85 mg/m\^2 IV q2w.
Paclitaxel
Participants will receive paclitaxel 200 mg/m\^2 IV q3w.
Pemetrexed
Participants will receive pemetrexed 500 mg/m\^2 IV q3w.
Laura and ISAAC Perlmutter Cancer Center at NYU Langone., New York
Georgetown University Medical Center Lombardi Cancer Center, Washington D.C.
Duke University Medical Center, Durham
Carolina BioOncology Institute; Can Therapy & Res Ctr, Huntersville
Sarah Cannon Research Inst., Nashville
Uni of Chicago, Chicago
University of Colorado Cancer Center, Aurora
Yale University, New Haven
Massachusetts General Hospital., Boston
Beth Israel Deaconess Med Ctr, Boston
Dana Farber Can Ins, Boston
Lead Sponsor
Genentech, Inc.
INDUSTRY